FDA recall record
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FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of May 21, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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Reason
During an FDA investigation the firm was notified that the product contains undeclared shellfish.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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Code information listed by FDA
LOT #2011216 EXP DATE 11/2022
Distribution and firm information
Recalling firm listed by FDA: NutraCap Labs LLC
Firm location listed by FDA: Norcross, GA, United States
Distribution reported by FDA: Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA & WA.
Product quantity listed by FDA: 80,169 various bottles and jars
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.